Class II · Moderate risk
PAPAVERINE HYDROCHLORIDE Injection
Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.
National Drug Code
Is NDC 72516-0024-10 recalled?
Papaverine Hydrochloride · 10 VIAL in 1 CARTON (72516-024-10) / 2 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 72516-0024-10 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Papaverine Hydrochloride
- Strength
- PAPAVERINE HYDROCHLORIDE 30 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Oryza Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 72516-0024
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Free recall alerts
Know the day your medication is recalled
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